Canonical Allele Identifier: PA2825399691
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1973555
ClinVar RCV Id: RCV002750579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035859.1:p.Ser211Gly
CA354627518
NM_001042400.3:c.631A>G